Advocacy and expertise for over 1 million people living with #MultipleSclerosis, NMOSD and MOGAD in Europe.

Brussels
Joined June 2012
European MS Platform retweeted
#MSToronto2026 Pre-Day is underway! Opening the third edition of Pre-Day, @ECTRIMS President Professor Bruno Stankoff highlighted the rapid progress taking place across the field and the importance of bringing experts together to address emerging scientific and clinical challenges. Today's programme features five sessions exploring: • Disease Mechanisms • Diagnostic Challenges • Prognosis and Outcomes Informed by Imaging and Fluid Biomarkers • Clinical Course and Outcomes • Treatment Approaches As our understanding of neuroimmunological diseases advances, so too does the need to explore where these conditions converge, where they differ and what these discoveries mean for diagnosis and treatment. Bringing together perspectives on MS, MOGAD, NMOSD, autoimmune encephalitis and other neuroinflammatory conditions, Pre-Day creates an important opportunity to exchange knowledge, strengthen collaboration and advance our collective understanding of neuroimmunology. 𝐄𝐱𝐩𝐥𝐨𝐫𝐞 𝐭𝐡𝐞 𝐩𝐫𝐨𝐠𝐫𝐚𝐦𝐦𝐞 ➡️ bit.ly/4yiNJd5 @ECTRIMS, @ACTRIMS, @MTCC_Events, @SeeTorontoNow #MSToronto2026 #MultipleSclerosis #Neurology #MSResearch
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European MS Platform retweeted
🌍 Don’t forget to join us at Patient Community Day on 23 Oct at 15:00 EDT. Engage with global experts, share your questions, and be part of the conversation driving MS research forward. 𝐒𝐢𝐠𝐧 𝐮𝐩 ➡️ bit.ly/44elQGb #ECTRIMS4me #PatientCommunityDay #MS #NMOSD #MOGAD
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European MS Platform retweeted
Just over one week to go until our Multiple Sclerosis Without Borders EU Webinar on 1 July. Join leading experts, policymakers and advocates to discuss the future of MS care, rights and research across Europe. Learn more: ms-society.ie/news/ms-withou…
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European MS Platform retweeted
🔍 𝐖𝐡𝐚𝐭 𝐜𝐡𝐚𝐥𝐥𝐞𝐧𝐠𝐞𝐬 𝐫𝐞𝐦𝐚𝐢𝐧 𝐢𝐧 𝐝𝐢𝐚𝐠𝐧𝐨𝐬𝐢𝐧𝐠 𝐌𝐎𝐆𝐀𝐃? Our latest Spotlight, 𝘔𝘖𝘎𝘈𝘋: 𝘌𝘮𝘦𝘳𝘨𝘪𝘯𝘨 𝘐𝘯𝘴𝘪𝘨𝘩𝘵𝘴 𝘢𝘯𝘥 𝘌𝘷𝘰𝘭𝘷𝘪𝘯𝘨 𝘊𝘩𝘢𝘭𝘭𝘦𝘯𝘨𝘦𝘴, explores the latest developments in MOGAD diagnosis, biomarkers, and therapeutic approaches. Read the Spotlight here: ectrims.eu/mogad-emerging-in… "While the criteria are a big step forward, obstacles remain in differentiating MOGAD from MS, which is crucial given the differences in treatment," says Professor Anne-Katrin Pröbstel of Universitätsklinikum Bonn and Universitätsspital Basel (USB). "A key unresolved question in MOGAD management is: how long do we treat people for, both after an initial attack and in those who experience relapses?" adds Dr. Wei Yeh of Monash University in Melbourne. The ECTRIMS Spotlight Series is curated and authored by our Scientific Content Writer, Stefania de Vito. #MultipleSclerosis #MOGAD #MSResearch #Neurology #MSSpotlight #Neuroimmunology #ECTRIMS
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European MS Platform retweeted
Honored to speak at #EMSP2026 in Berlin on “Not just a label: a biology-driven approach that fits you.” A special moment for me, sharing why care should adapt to the person, not the other way around. 💪🏻
"We need to go further than biomarkers when it comes to monitoring the disease" Interesting session on going beyond biology. Streaming now- eu-admin.eventscloud.com/web… @PPuljic92
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European MS Platform retweeted
👏 Congratulations to Dr Kristen Krysko, winner of the 2025 #RachelHornePrize for Women’s Research in MS. She is recognised for her pioneering research into how best to guide and treat women with MS during pregnancy and breastfeeding. 🔗 msintfederation.org/3UT0H03 #MSResearch
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European MS Platform retweeted
📢1 month to go until #EAN2025! Join us in Helsinki for the 11th Annual EAN Congress! Submit your membership applications before 31 May for reduced rates - don't miss out on this opportunity! #EANeurology Learn more about the EBC sessions & register now👉braincouncil.eu/event/ean-co…
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European MS Platform retweeted
“I didn’t have many opportunities to speak with other young people living with MS.” – Anna Revilla That changed in 2022 when she joined @eumsplatform Young People’s Network, and even bigger changes followed in 2025. Read Anna's guest blog here: ms-society.ie/ms-and-me/e-em…
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European MS Platform retweeted
The #EBVMS Annual Consortium meeting starts today! ⚡️We are diving into clinical trials, AI, data updates, and stakeholder engagement to advance #MS research! Stay tuned for updates 🧠 #HorizonEU #HaDEA #EBV
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European MS Platform retweeted
📢 Excited to attend #ECF2024 in Baveno, Italy (Nov 21–23)! This year’s theme: "Changes in MS in the Past 25 Years: Impact on Treatment" promises groundbreaking discussions on MS care & research @eumsplatform #EMSP #ECF2024 #MSAwareness #MultipleSclerosis
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European MS Platform retweeted
#Accessibility is about removing barriers in every area of life. This month in our #DisabilityVoice: ➡️Accessible communication ➡️The role of standards in accessibility ➡️Challenges for travellers with disabilities ➡️Accessibility in sustainability mailchi.mp/edf-feph/dv2024-c…
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European MS Platform retweeted
#Women with #MS face unique challenges, such as #reproductive issues and #menopause. Read the recap of our recent 3webinar feat. experts from @ClevelandClinic @cemcat_em & @DalhousieU as they discuss where research should focus its efforts first ➡️ bit.ly/48Sulsk
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European MS Platform retweeted
Persons with disabilities are among the hardest hit by climate change. Ahead of #COP29, we call on negotiators to recognise their voices by establishing a Disability Constituency. Our press release: buff.ly/40A3IXa #DisabilityInclusion #ClimateActionNow
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European MS Platform retweeted
🌍 Join the @PromsInitiative Annual Meeting on 20 November! The session is on ‘Digital Science of People with MS Input in the Era of Personalised Medicine.’ 💻 Learn more and register now to be part of the discussion on shaping the future of MS care. 👉 msintfederation.org/3UCyydK
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European MS Platform retweeted
Researchers looking for the causes of #MS should factor in the prodromal phase, says Prof. Helen Tremlett of @UBC. In our latest #podcast, Brett Drummond of @MSTranslate explores what the MS prodrome means for diagnosis & treatment. Listen now! 👉 bit.ly/4hvgUCy
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European MS Platform retweeted
🚀 Happening today! It's not too late to join our free #webinar focusing on the unmet needs of women with #MS at 18:30-19:30 CET. Featuring experts from @cemcat_em, @ClevelandClinic & @DalhousieU. Register here! ➡️ bit.ly/48HlVUR
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European MS Platform retweeted
🔎 Research shows that about half of all side effects are preventable! This #MedSafetyWeek, we urge healthcare professionals to prescribe medicine with care & #ReportSideEffects. Your reports help regulators like the EMA monitor risks & ensure safer medicines. 🫂💊
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European MS Platform retweeted
MSIF has signed an open letter to world leaders, urging all governments to fulfil their commitments to address the burden of noncommunicable diseases (NCDs) - including MS. 📣 Read the letter here: msintfederation.org/ncd #ActonNCDs #LeadonNCDs @ncdalliance
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European MS Platform retweeted
The @Europarl_EN's Disability Intergroup must be re-established! Our new video shows the impact of the Intergroup in advancing #DisabilityRights. #EPDisability Learn more:edf-feph.org/disability-inte… @k_langensiepen @ChiaraGemmaUE @joseggusmao @MaxovaRadka @adamkosamep
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